Device recall
Z-0556-2016: Granada Biphasic Broth The product is a selective medium for the screening and…
FDA device recall · Class II · Biomerieux Inc
Key facts
| Recall number (Z-number) | Z-0556-2016 |
|---|---|
| Recall event | 72760 |
| Product | Granada Biphasic Broth The product is a selective medium for the screening and identification of Streptococcus agalactiae in pregnant women using clinical specimens. |
| Product code | NJR |
| Recalling firm | Biomerieux Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 24, 2016 |
| FEI number | 1950204 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database